Drug recall
Source Plasma
FDA recall event 26172 · Class III · Biomat USA, Inc
Key facts
| Event ID | 26172 |
|---|---|
| Recall numbers | B-1080-3 |
| Recalling firm | Biomat USA, Inc |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class III |
| Status | Completed |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, collected from a donor whose arm inspection was not documented, was distributed. |
| Initiation date | Jan 4, 2002 |
| City | Houston |
| Country | United States |
| FEI number | 1643531 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports